Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.

Although recent publications have linked the molecular events driving facioscapulohumeral muscular dystrophy (FSHD) to expression of the double homeobox transcription factor DUX4, overexpression of FRG1 has been proposed as one alternative causal agent as mice overexpressing FRG1 present with muscul...

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Main Authors: Steven C Chen, Ellie Frett, Joseph Marx, Darko Bosnakovski, Xylena Reed, Michael Kyba, Brian K Kennedy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3095625?pdf=render
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spelling doaj-d5bbcfa0dd4f45648f50f3e4aab60b9e2020-11-25T02:54:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e1978010.1371/journal.pone.0019780Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.Steven C ChenEllie FrettJoseph MarxDarko BosnakovskiXylena ReedMichael KybaBrian K KennedyAlthough recent publications have linked the molecular events driving facioscapulohumeral muscular dystrophy (FSHD) to expression of the double homeobox transcription factor DUX4, overexpression of FRG1 has been proposed as one alternative causal agent as mice overexpressing FRG1 present with muscular dystrophy. Here, we characterize proliferative defects in two independent myoblast lines overexpressing FRG1. Myoblasts isolated from thigh muscle of FRG1 transgenic mice, an affected dystrophic muscle, exhibit delayed proliferation as measured by decreased clone size, whereas myoblasts isolated from the unaffected diaphragm muscle proliferated normally. To confirm the observation that overexpression of FRG1 could impair myoblast proliferation, we examined C2C12 myoblasts with inducible overexpression of FRG1, finding increased doubling time and G1-phase cells in mass culture after induction of FRG1 and decreased levels of pRb phosphorylation. We propose that depressed myoblast proliferation may contribute to the pathology of mice overexpressing FRG1 and may play a part in FSHD.http://europepmc.org/articles/PMC3095625?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Steven C Chen
Ellie Frett
Joseph Marx
Darko Bosnakovski
Xylena Reed
Michael Kyba
Brian K Kennedy
spellingShingle Steven C Chen
Ellie Frett
Joseph Marx
Darko Bosnakovski
Xylena Reed
Michael Kyba
Brian K Kennedy
Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.
PLoS ONE
author_facet Steven C Chen
Ellie Frett
Joseph Marx
Darko Bosnakovski
Xylena Reed
Michael Kyba
Brian K Kennedy
author_sort Steven C Chen
title Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.
title_short Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.
title_full Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.
title_fullStr Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.
title_full_unstemmed Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.
title_sort decreased proliferation kinetics of mouse myoblasts overexpressing frg1.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Although recent publications have linked the molecular events driving facioscapulohumeral muscular dystrophy (FSHD) to expression of the double homeobox transcription factor DUX4, overexpression of FRG1 has been proposed as one alternative causal agent as mice overexpressing FRG1 present with muscular dystrophy. Here, we characterize proliferative defects in two independent myoblast lines overexpressing FRG1. Myoblasts isolated from thigh muscle of FRG1 transgenic mice, an affected dystrophic muscle, exhibit delayed proliferation as measured by decreased clone size, whereas myoblasts isolated from the unaffected diaphragm muscle proliferated normally. To confirm the observation that overexpression of FRG1 could impair myoblast proliferation, we examined C2C12 myoblasts with inducible overexpression of FRG1, finding increased doubling time and G1-phase cells in mass culture after induction of FRG1 and decreased levels of pRb phosphorylation. We propose that depressed myoblast proliferation may contribute to the pathology of mice overexpressing FRG1 and may play a part in FSHD.
url http://europepmc.org/articles/PMC3095625?pdf=render
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